Human Genome Epidemiology Literature Finder
Records 1 - 15 (of 15 Records) |
Query Trace: Syndrome and MTOR[original query] |
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DAXX/ATRX, MEN1, and mTOR pathway genes are frequently altered in pancreatic neuroendocrine tumors. Science (New York, N.Y.) 2011 1 331 (6021): 1199-203. Jiao Yuchen, Shi Chanjuan, Edil Barish H, de Wilde Roeland F, Klimstra David S, Maitra Anirban, Schulick Richard D, Tang Laura H, Wolfgang Christopher L, Choti Michael A, Velculescu Victor E, Diaz Luis A, Vogelstein Bert, Kinzler Kenneth W, Hruban Ralph H, Papadopoulos Nickol |
Pulmonary Neoplasms in Patients with Birt-Hogg-Dubé Syndrome: Histopathological Features and Genetic and Somatic Events. PloS one 2016 11 (3): e0151476. Furuya Mitsuko, Tanaka Reiko, Okudela Koji, Nakamura Satoko, Yoshioka Hiromu, Tsuzuki Toyonori, Shibuya Ryo, Yatera Kazuhiro, Shirasaki Hiroki, Sudo Yoshiko, Kimura Naoko, Yamada Kazuaki, Uematsu Shugo, Kunimura Toshiaki, Kato Ikuma, Nakatani Yuk |
Association of genetic polymorphisms of angiopoietin-like 4 with severity of posttransplant proteinuria in kidney allograft recipients. Transplant immunology 2016 Nov . Chang Youngil, Shah Tariq, Yang Jaewook, Min David |
Clinical manifestations and STK11 germline mutations in Taiwanese patients with Peutz-Jeghers syndrome. Asian journal of surgery 2017 9 41 (5): 480-485. Chiang Jy-Ming, Chen Tse-Chi |
The efficacy of everolimus and sunitinib in patients with sporadic or germline mutated metastatic pancreatic neuroendocrine tumors. Journal of gastrointestinal oncology 2019 8 10 (4): 645-651. Nuñez Jose Eduardo, Donadio Mauro, Filho Duilio Rocha, Rego Juliana Florinda, Barros Milton, Formiga Maria Nirvana, Lopez Rossana, Riechelmann Rach |
ONCOGENE PANEL SEQUENCING ANALYSIS IDENTIFIES CANDIDATE ACTIONABLE GENES IN ADVANCED WELL-DIFFERENTIATED GASTROENTEROPANCREATIC NEUROENDOCRINE TUMORS. Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists 2019 3 25 (6): 580-588. Tirosh Amit, Killian J Keith, Zhu Yuelin Jack, Petersen David, Walling Jennifer, Mor-Cohen Ronit, Neychev Vladimir, Stevenson Holly, Keutgen Xavier M, Patel Dhaval, Nilubol Naris, Meltzer Paul, Kebebew Electr |
Associations of CDH1 germline variant location and cancer phenotype in families with hereditary diffuse gastric cancer (HDGC). Journal of medical genetics 2019 2 56 (6): 370-379. Lo Winifred, Zhu Bin, Sabesan Arvind, Wu Ho-Hsiang, Powers Astin, Sorber Rebecca A, Ravichandran Sarangan, Chen Ina, McDuffie Lucas A, Quadri Humair S, Beane Joal D, Calzone Kathleen, Miettinen Markku M, Hewitt Stephen M, Koh Christopher, Heller Theo, Wacholder Sholom, Rudloff U |
Association of a genetic variant in AKT1 gene with features of the metabolic syndrome. Genes & diseases 2019 Sep 6 (3): 290-295. Eshaghi Fateme Sadat, Ghazizadeh Hamideh, Kazami-Nooreini Sakine, Timar Ameneh, Esmaeily Habibollah, Mehramiz Mehrane, Avan Amir, Ghayour-Mobarhan Maj |
Serine/Threonine Kinase 11 Plays a Canonical Role in Malignant Progression of KRAS -Mutant and GNAS -Wild-Type Intraductal Papillary Mucinous Neoplasms of the Pancreas. Annals of surgery 2021 4 277 (2): e384-e395. Omori Yuko, Ono Yusuke, Morikawa Takanori, Motoi Fuyuhiko, Higuchi Ryota, Yamamoto Masakazu, Hayakawa Yuko, Karasaki Hidenori, Mizukami Yusuke, Unno Michiaki, Furukawa To |
Comprehensive Molecular Characterization and Response to Therapy in Fumarate Hydratase-Deficient Renal Cell Carcinoma. Clinical cancer research : an official journal of the American Association for Cancer Research 2021 3 27 (10): 2910-2919. Gleeson Jack P, Nikolovski Ines, Dinatale Renzo, Zucker Mark, Knezevic Andrea, Patil Sujata, Ged Yasser, Kotecha Ritesh R, Shapnik Natalie, Murray Samuel, Russo Paul, Coleman Jonathan, Lee Chung Han, Stadler Zsofia K, Hakimi A Ari, Feldman Darren R, Motzer Robert J, Reznik Ed, Voss Martin H, Chen Ying-Bei, Carlo Maria |
Lynch syndrome pre-screening and comprehensive characterization in a multi-center large cohort of Chinese patients with colorectal cancer. Cancer biology & medicine 2022 5 19 (8): 1235-48. Li Yan, Fan Lihong, Zheng Jianming, Nie Xiu, Sun Yu, Feng Qin, Lian Shenyi, Bai Wenqi, Cai Weijing, Yang Yanan, Su Bo, Xi Yanfeng, Lin Dongm |
Targeted next-generation sequencing for detection of PIK3CA mutations in archival tissues from patients with Klippel-Trenaunay syndrome in an Asian population : List the full names and institutional addresses for all authors. Orphanet journal of rare diseases 2023 9 18 (1): 270. Yuki Sasaki, Kosuke Ishikawa, Kanako C Hatanaka, Yumiko Oyamada, Yusuke Sakuhara, Tadashi Shimizu, Tatsuro Saito, Naoki Murao, Tomohiro Onodera, Takahiro Miura, Taku Maeda, Emi Funayama, Yutaka Hatanaka, Yuhei Yamamoto, Satoru Sasa |
Genetic variations in a Sestrin2/Sestrin3/mTOR Axis and development of new-onset diabetes after kidney transplantation. Transplant immunology 2023 11 81 101947. Don Luu, Tariq Shah, Prashant Sakharkar, David I M |
MTOR gene variants are associated with severe COVID-19 outcomes: A multicenter study. International immunopharmacology 2023 11 125 (Pt B): 111155. Bruna Ramos Tosta, Ingrid Marins de Almeida, Laiane da Cruz Pena, Hatilla Dos Santos Silva, Fabiane S Reis-Goes, Nívia N Silva, João Victor Andrade Cruz, Mailane Dos Anjos Silva, Jéssica Francisco de Araújo, Juliana Lopes Rodrigues, Gabriella Oliveira, Ricardo Gassmann Figueiredo, Sara Nunes Vaz, Iris Montaño-Castellón, Daniele Santana, Fabyan Esberard de Lima Beltrão, Valdirene Leão Carneiro, Gubio Soares Campos, Carlos Brites, Vitor Fortuna, Camila Alexandrina Figueiredo, Soraya Castro Trindade, Helton Estrela Ramos, Ryan Dos Santos Cos |
Impulsivity and aggression in alcohol withdrawal syndrome is modulated by the interaction of ZNF804A and mTOR polymorphism. Pharmacology, biochemistry, and behavior 2024 1 236 173708. Guanghui Shen, Yuyu Wu, Kexin Wang, Michelle Niculescu, Yuqing Liu, Yimin Kang, Xingguang Luo, Wei Wang, Yu-Hsin Chen, Yanlong Liu, Fan Wang, Li Ch |
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